Academic literature on the topic 'N-chloro derivatives'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'N-chloro derivatives.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "N-chloro derivatives"

1

K. Abdullah, Ebtihal. "Synthesis of New (1-alkylamino-4-phenyldithio-2-bntanol amine) andderivatives." Tikrit Journal of Pharmaceutical Sciences 6, no. 1 (2023): 78–82. http://dx.doi.org/10.25130/tjphs.2010.6.1.12.78.82.

Full text
Abstract:
Anew series of(1-alkylamino-4-phenyldithio-2-bntanol amine) and derivatives,containing two functional groups (pheny ring and NCS2) here been prepared from a reaction by 3steps :- 1-In the first step the preparation of n-phenyl dithio carbamate (A) and derivatives from a reaction between Aniline and carbon disulfide in basic medium. 2-Then , preparation N-3-chloro-2-hydroxy propyl amine tt 3 )) and derivativel from reaction between N-3-chloro-2-hydroxy propylamine and epichloro hydrine in methanolic a queous.3-In three step :-preparation 1-Alkyi amino -4-phenyl dithio-2-butanol amine ( I-IV) fr
APA, Harvard, Vancouver, ISO, and other styles
2

C., B. Rajashekar Reddy, Rajasekhara Reddy Sabbasani, Shivaji Naidu, Muralidhar B., and Jayachandra R. "An improved, practical and efficient method for the synthesis of novel N-chloro derivatives using calcium hypochlorite." Journal of Indian Chemical Society Vol. 92, Jun 2015 (2015): 847–50. https://doi.org/10.5281/zenodo.5636284.

Full text
Abstract:
Organic Chemistry Division, Department of Chemistry, VIT University, Vellore-632 014, Tamilnadu, India <em>E-mail</em> : sekharareddy@vit.ac.in, sekharareddyiitm@gmail.com The developed method was employed in the synthesis of medicinally important compounds and intermediates in the organic synthesis. Herein we report a variety of novel <em>N</em>-chloro derivatives of benzisoxazole, benzimidazoles and several other <em>N</em>-chloro derivatives using 1.2 equivalents of calcium hypochlorite. The process does not require any additives like acids or bases and produced moderate to excellent yields
APA, Harvard, Vancouver, ISO, and other styles
3

Rádl, Stanislav, and Lenka Kovářová. "Some reactions of N-propadienyl-4-quinolones." Collection of Czechoslovak Chemical Communications 56, no. 11 (1991): 2413–19. http://dx.doi.org/10.1135/cccc19912413.

Full text
Abstract:
N-Alkylation of ethyl 6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (Vg) with 3-bromopropyne followed by acidic hydrolysis provided N-propyl derivative Ic which in alkaline media yielded N-propadienyl derivative IId. Propadienyl derivatives IIa and IIb treated with primary or secondary amines provided intermediates IIIa-IIIc which were hydrolyzed to N-acetonyl derivatives IVa and IVb, respectively. N-Benzylation of ethyl 7-chloro-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (Va) followed by hydrolysis yielded 1-benzyl-7-chloro-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic ac
APA, Harvard, Vancouver, ISO, and other styles
4

Dillip, Kumar Ojha, N. Prasad R., Rao Hitesh, Gupta Yogesh, Agrawal Umesh, and Chand Pooran. "Adenosine receptors. Part 1 : (2S,3S,4R,5R)-2-(4-(alkyl/arylamino)-5Hpyrrolo[3,2-d]pyrimidin-7-yl)-5-(hydroxymethyl)pyrrolidine-3,4-diol derivatives as possible adenosine receptor agonists." Journal of Indian Chemical Society Vol. 91, Aug 2014 (2014): 1451–57. https://doi.org/10.5281/zenodo.5728670.

Full text
Abstract:
Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India Therachem Research Medilab (Ind) Pvt. Ltd., E 969, Biotechnology Park, Sitapura Industrial Area, Jaipur-302 022, Rajasthan, India <em>E-mail</em> : ojha79@gmail.com, pchand@therachemlab.com, rnp_1949@yahoo.co.in <em>Manuscript received 19 January 2014, accepted 01 February 2014</em> 6-Substitued adenosine derivatives are well known adenosine receptor agonists and a few of these derivatives are being used as therapeutic agents. A series of novel N<sup>6</sup> -substituted-9-deaza adenosine or N<sup>4</sup> -subst
APA, Harvard, Vancouver, ISO, and other styles
5

Callebaut, Gert, Sven Mangelinckx, Pieter Van der Veken, Karl W. Törnroos, Koen Augustyns та Norbert De Kimpe. "Asymmetric synthesis of γ-chloro-α,β-diamino- and β,γ-aziridino-α-aminoacylpyrrolidines and -piperidines via stereoselective Mannich-type additions of N-(diphenylmethylene)glycinamides across α-chloro-N-sulfinylimines". Beilstein Journal of Organic Chemistry 8 (5 грудня 2012): 2124–31. http://dx.doi.org/10.3762/bjoc.8.239.

Full text
Abstract:
The asymmetric synthesis of new chiral γ-chloro-α,β-diaminocarboxylamide derivatives by highly diastereoselective Mannich-type reactions of N-(diphenylmethylene)glycinamides across chiral α-chloro-N-p-toluenesulfinylaldimines was developed. The resulting (S S,2S,3S)-γ-chloro-α,β-diaminocarboxylamides were formed with the opposite enantiotopic face selectivity as compared to the (S S,2R,3R)-γ-chloro-α,β-diaminocarboxyl esters obtained via Mannich-type addition of analogous N-(diphenylmethylene)glycine esters across a chiral α-chloro-N-p-toluenesulfinylaldimine. Selective deprotection under diff
APA, Harvard, Vancouver, ISO, and other styles
6

Marsden, Helen M., and Jean'ne M. Shreeve. "Sulfur derivatives of N-chloro compounds." Journal of Fluorine Chemistry 29, no. 1-2 (1985): 35. http://dx.doi.org/10.1016/s0022-1139(00)83270-4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Šindelář, Karel, Vladimír Valenta, Jiří Holubek, Oluše Matoušová, and Miroslav Protiva. "Potential antidepressants. Synthesis of 6,11-dihydrodibenzo[b,e]thiepin-11-yl (dimethylaminomethyl)phenyl ethers, sulfides, amines and some related compounds." Collection of Czechoslovak Chemical Communications 55, no. 1 (1990): 282–95. http://dx.doi.org/10.1135/cccc19900282.

Full text
Abstract:
Reactions of 11-chloro-6,11-dihydrodibenzo[b,e]thiepin and its 2-bromo derivative with the isomeric (dimethylaminomethyl)phenols, (dimethylaminomethyl)thiophenols, and (dimethylaminomethyl)anilines in toluene afforded the title compounds IIIb,c, Va, VIIIa,b,c, and Xa,b,c. Reactions of 11-chloro-6,11-dihydrodibenzo[b,e]thiepin and its 2-chloro and 2-methyl derivatives with N,N-dimethyl-2-(4-aminophenoxy)ethylamine and N,N-dimethyl-3-(4-aminophenoxy)propylamine by heating in dimethylformamide in the presence of sodium carbonate gave the diamino ethers XI-XIV. The compounds showed only indication
APA, Harvard, Vancouver, ISO, and other styles
8

Olszewska, E., B. Tarasiuk, and S. Pikus. "New powder diffraction data of some N-derivatives of 4-chloro-3,5-dimethylphenoxyacetamide-potential pesticides." Powder Diffraction 26, no. 4 (2011): 337–45. http://dx.doi.org/10.1154/1.3652921.

Full text
Abstract:
N-derivatives of 4-chloro-3,5-dimethylphenoxyacetamide—2-(4-chloro-3,5-dimethylphenoxy)-N-(4-fluorophenyl)acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-(3-chloro-4-fluorophenyl) acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-[4-chloro-3-(trifluoromethyl)phenyl] acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-[3-chloro-4-methylphenyl]acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-(2,4,6-tribromophenyl) acetamide, 2-(4-chloro-3,5-dimethylphenoxy)-N-pyridin-2-ylacetamide, 1-[(4-chloro-3,5-dimethylphenoxy)acetyl]-4-methylpiperazine, and 1-benzyl-4-[(4-chloro-3,5-dimethylphenoxy)acetyl]piperazine—have
APA, Harvard, Vancouver, ISO, and other styles
9

Hoogeveen, A. P. J. "Derivatives of n-hexylamine with chloro-dinitro- and chloro-trinitronaphthalenes." Recueil des Travaux Chimiques des Pays-Bas 46, no. 12 (2010): 918–21. http://dx.doi.org/10.1002/recl.19270461210.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Tudose, Madalina, Florin Badea, Miron Caproiu, et al. "New N-aryloxy-phthalimide derivatives. Synthesis, physico-chemical properties, and QSPR studies." Open Chemistry 8, no. 4 (2010): 789–96. http://dx.doi.org/10.2478/s11532-010-0063-6.

Full text
Abstract:
AbstractStarting from N-hydroxyphthalimide 1 and the reactive fluoro- or chloro-nitroaryl derivatives 2, 3 and 4a-e (2-chloro-3,5-dinitropyridine; 3, NBD-chloride; 4a, 1-fluoro-2,4-dinitrobenzene; 4b, picryl chloride; 4c, 4-chloro-3,5-dinitrobenzotrifluoride; 4d, 2-chloro-3,5- dinitrobenzotrifluoride; 4e, 4-chloro-3,5-dinitrobenzoic acid) the corresponding N-(2-nitroaryloxy)-phthalimide derivatives 5a-e, or 6 and 7 were obtained and characterized by IR, UV-Vis 1H-NMR and 13C-NMR spectroscopy. The TLC behavior and the hydrophobicity of these derivatives have been experimentally evaluated by RM0
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "N-chloro derivatives"

1

Shtamburg, V. G., A. V. Tsyhankov, V. V. Shtamburg, et al. "1-(N-Alkoxyamino)pyridine Derivatives and others N-Alkoxyhydrazines." Thesis, Ekskluziv Publ, 2015. http://repository.kpi.kharkov.ua/handle/KhPI-Press/36899.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Sharma, Prawin Kumar. "Greener approach to the synthesis of some novel class of isoxazolidine and isoxazoline derivatives using N-methyl and N-phenyl-a-chloro nitrones." Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/1884.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Tan, Chao-Yuan, and 譚朝元. "Solution-Processed N-type Microribbon Field-Effect Transistors Based on Chloro-Substituted Perylene Diimides Derivatives." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/18422824887047869134.

Full text
Abstract:
碩士<br>國立交通大學<br>照明與能源光電研究所<br>105<br>This study employed a chloro-substituted perylene diimides derivative (Cl-PEPTC) for the formation of self-assembled single crystal micoribbons by solvent exchange method. Transistor devices based on a network of Cl-PEPTC microribbions have showed typical n-channel field-effect behaviors. The extracted maxima mobility was 1.05 × 10-3 cm2V-1s-1, threshold voltage was 68.3 V and on/off current ratio was 4.74 × 104. The devices were further measured under three different conditions: (ⅰ) glove box, (ⅱ) ambient air (relative humidity 50 – 60 %) and (ⅲ) high humi
APA, Harvard, Vancouver, ISO, and other styles
4

KUO, YUAN-TSUNG, and 郭原宗. "Kinetic Studies of Type II Photoinitiator Photopolymerization Based on 2-Chloro-hexaarylbimmidazole (o-Cl-HABI)/N-Phenyl glycine (NPG) and Its Derivatives." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/27mms6.

Full text
Abstract:
碩士<br>國立高雄應用科技大學<br>化學工程與材料工程系博碩士班<br>106<br>Type II photoinitiator systems are widely used in photocuring processes due to their low cost, faster photospeed which applied in many industrial applications such as photoresist dry film and imaging. One of the typical Type II photo-initiator package based on o-Cl-HABI (hydrogen acceptor) and NPG (hydrogen donor) systems (where o-Cl-HABI is a 2-chlorohexaaryl biimidazole, NPG is an N-phenyl glycine) was investigated in this study. The photocuring behavior for different weight ratios of o-Cl-HABI and NPG was studied through FT-IR, gel-fraction, elec
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "N-chloro derivatives"

1

Lacherai, A., R. De Jaeger, A. Mazzah, C. Fournier, and B. Hecquet. "Spectroscopic Study of N,N,-bis(chloro-2 Ethyl)Amino Derivatives of HN(P(O)Cl2)2. Application to the Synthesis of Compounds Exhibiting Antitumoral Activity." In Spectroscopy of Biological Molecules. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_242.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

"Study of light-induced interaction of quinone derivatives with guanosine and guanosine-rich oligonucleotides." In Book of Abstracts - RAD 2025 Conference. RAD Centre, Niš, Serbia, 2025. https://doi.org/10.21175/rad.abstr.book.2025.6.3.

Full text
Abstract:
Quinones are a broad class of compounds of both synthetic and natural origin that are actively used in medicine, particularly in anticancer therapy. Their main mechanism of cytotoxicity is associated with interaction with DNA. This type of interaction is possible due to the flat aromatic system of quinones. Model processes of interaction of the naphthoquinone derivative N-(2-chloro-1,4- naphthoquinonyl)-b-alanine (Nap) as well as the anthraquinone 2-phenyl-4-(butylamino)- naphtholquinoline-7,12-dione (Q1) with 5'-guanidylic acid (GMP) and oligonucleotide sequences of different lengths (2G, 3G,
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "N-chloro derivatives"

1

Bułakowska, Anita, Jarosław Sławiński, and Rafał Hałasa. "Evaluation of the Antimicrobial Activity of N-Acylated 4-Chloro-2-mercaptobenzenesulfonamide Derivatives." In ECMC 2022. MDPI, 2022. http://dx.doi.org/10.3390/ecmc2022-13289.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Simijonović, Dušica, Marko Antonijević, Edina Avdović, Zorica Petrović, and Zoran Marković. "INHIBITORY EFFECT OF COUMARIN BENZOYLHYDRAZONES ON MCL-1 PROTEIN." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.442s.

Full text
Abstract:
The protein that controls cell differentiation in acute myeloid leukemia is MCL-1. High-level of this protein causes the carcinogenesis. In this paper inhibitory effect of two coumarin benzoylhydrazones,(E)-2-hydroxy-N’-(1-(2-oxo-2H-chromen-3-yl)ethylidene)benzohydrazide (A) and (E)-4-hydroxy-N’-(1-(2-oxo-2H-chromen-3-yl)ethylidene)benzohydrazide (B) against MCL-1 protein was investigated. For this purpose, a molecular docking simulations were used. The obtained results showed that compound A showed better activity than compound B. Also, the docking simulations against MCL-1 protein were perfo
APA, Harvard, Vancouver, ISO, and other styles
3

Sucman, Natalia. "Diastereoselective synthesis of a novel cyclic derivative based on 2,3-indolinedione." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab18.

Full text
Abstract:
Generally, organic synthesis is renowned for its predictability in determining results. Nevertheless, there are situations where instead of the expected products, unexpected compounds with unique structures may arise. This report is a presentation of one such remarkable cyclic compound with four chiral centres prepared by diastereoselective dimerization of Morita-Baylis-Hillman (MBH) adducts of acrylonitrile to 5-chloro-indole-2,3dione. MBH adducts are very popular in organic chemistry. They are synthesized by the addition of an activated alkene and a carbon electrophile in the presence of a n
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!